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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1995 1
1996 1
1997 4
1998 1
2000 2
2001 1
2002 3
2004 2
2005 2
2007 1
2009 1
2012 1
2013 1
2014 2
2015 3
2016 3
2017 3
2018 1
2019 2
2023 1
2024 0

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32 results

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Page 1
RNA-binding proteins in neurological diseases.
Zhou H, Mangelsdorf M, Liu J, Zhu L, Wu JY. Zhou H, et al. Among authors: mangelsdorf m. Sci China Life Sci. 2014 Apr;57(4):432-44. doi: 10.1007/s11427-014-4647-9. Sci China Life Sci. 2014. PMID: 24658850 Free article. Review.
Transgenic mice overexpressing mutant TDP-43 show aberrant splicing of neurological disorders-associated gene Zmynd11 prior to onset of motor symptoms.
Narayanan RK, Panwar A, Butler TJ, Cutrupi AN, Kennerson M, Vucic S, Ashokkumar B, Mangelsdorf M, Wallace RH. Narayanan RK, et al. Among authors: mangelsdorf m. MicroPubl Biol. 2023 Mar 14;2023:10.17912/micropub.biology.000777. doi: 10.17912/micropub.biology.000777. eCollection 2023. MicroPubl Biol. 2023. PMID: 37008727 Free PMC article.
Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis.
Benyamin B, He J, Zhao Q, Gratten J, Garton F, Leo PJ, Liu Z, Mangelsdorf M, Al-Chalabi A, Anderson L, Butler TJ, Chen L, Chen XD, Cremin K, Deng HW, Devine M, Edson J, Fifita JA, Furlong S, Han YY, Harris J, Henders AK, Jeffree RL, Jin ZB, Li Z, Li T, Li M, Lin Y, Liu X, Marshall M, McCann EP, Mowry BJ, Ngo ST, Pamphlett R, Ran S, Reutens DC, Rowe DB, Sachdev P, Shah S, Song S, Tan LJ, Tang L, van den Berg LH, van Rheenen W, Veldink JH, Wallace RH, Wheeler L, Williams KL, Wu J, Wu X, Yang J, Yue W, Zhang ZH, Zhang D, Noakes PG, Blair IP, Henderson RD, McCombe PA, Visscher PM, Xu H, Bartlett PF, Brown MA, Wray NR, Fan D. Benyamin B, et al. Among authors: mangelsdorf m. Nat Commun. 2017 Sep 20;8(1):611. doi: 10.1038/s41467-017-00471-1. Nat Commun. 2017. PMID: 28931804 Free PMC article.
What does Australia's investment in genomics mean for public health?
Belcher A, Mangelsdorf M, McDonald F, Curtis C, Waddell N, Hussey K. Belcher A, et al. Among authors: mangelsdorf m. Aust N Z J Public Health. 2019 Jun;43(3):204-206. doi: 10.1111/1753-6405.12887. Epub 2019 Mar 4. Aust N Z J Public Health. 2019. PMID: 30830712 Free article. No abstract available.
C9orf72 hexanucleotide repeat expansions in Chinese sporadic amyotrophic lateral sclerosis.
He J, Tang L, Benyamin B, Shah S, Hemani G, Liu R, Ye S, Liu X, Ma Y, Zhang H, Cremin K, Leo P, Wray NR, Visscher PM, Xu H, Brown MA, Bartlett PF, Mangelsdorf M, Fan D. He J, et al. Among authors: mangelsdorf m. Neurobiol Aging. 2015 Sep;36(9):2660.e1-8. doi: 10.1016/j.neurobiolaging.2015.06.002. Epub 2015 Jun 9. Neurobiol Aging. 2015. PMID: 26142124
Multiplex families with epilepsy: Success of clinical and molecular genetic characterization.
Afawi Z, Oliver KL, Kivity S, Mazarib A, Blatt I, Neufeld MY, Helbig KL, Goldberg-Stern H, Misk AJ, Straussberg R, Walid S, Mahajnah M, Lerman-Sagie T, Ben-Zeev B, Kahana E, Masalha R, Kramer U, Ekstein D, Shorer Z, Wallace RH, Mangelsdorf M, MacPherson JN, Carvill GL, Mefford HC, Jackson GD, Scheffer IE, Bahlo M, Gecz J, Heron SE, Corbett M, Mulley JC, Dibbens LM, Korczyn AD, Berkovic SF. Afawi Z, et al. Among authors: mangelsdorf m. Neurology. 2016 Feb 23;86(8):713-22. doi: 10.1212/WNL.0000000000002404. Epub 2016 Jan 22. Neurology. 2016. PMID: 26802095 Free PMC article.
Protecting trust in medical genetics in the new era of forensics.
Curtis C, Hereward J, Mangelsdorf M, Hussey K, Devereux J. Curtis C, et al. Among authors: mangelsdorf m. Genet Med. 2019 Jul;21(7):1483-1485. doi: 10.1038/s41436-018-0396-7. Epub 2018 Dec 18. Genet Med. 2019. PMID: 30559376 Free PMC article. No abstract available.
Dynamic mutation loci: allele distributions in different populations.
Richards RI, Crawford J, Narahara K, Mangelsdorf M, Friend K, Staples A, Denton M, Easteal S, Hori TA, Kondo I, Jenkins T, Goldman A, Panich V, Ferakova E, Sutherland GR. Richards RI, et al. Among authors: mangelsdorf m. Ann Hum Genet. 1996 Sep;60(5):391-400. doi: 10.1111/j.1469-1809.1996.tb00437.x. Ann Hum Genet. 1996. PMID: 8912792
32 results